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FDA, SNM and RSNA host April 13-14 two-topic imaging workshop
Date:4/1/2010

of PET drugs in December 2009. The new regulations, known as 21 CFR Part 212, take effect on Dec. 12, 2011. All PET drug manufacturers will be required to submit a new or abbreviated drug application for PET drugs in commercial/clinical use by that date. In the interim, U.S. facilities must continue to comply with USP General Chapter <823>, which sets standards for the production of PET drugs.

The workshop is free and open to the public. However, early registration is encouraged as space is limited. To register, please visit www.rsna.org/snm/index.html.


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Contact: Amy Shaw
ashaw@snm.org
703-652-6773
Society of Nuclear Medicine
Source:Eurekalert

Page: 1 2

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